Clinical research - Articles

Discover how Clinion's Electronic Trial Master File (eTMF) optimizes clinical trial management with secure, efficient, and compliant document handling
Ensure faster trials, regulatory compliance, and real-time oversight with Clinion's innovative eTMF software. In the dynamic world of clinical research, efficient management of data and documents is crucial. Clinion's Electronic Trial Master File (eTMF) simplifies this process by providing a centralized platform for storing, organizing, and tracking all your clinical trial essentials. Key Benefits:Rapid Deployment: Start quickly with pre-built models and a configurable structure, reducing setup time to weeks. Intuitive Interface: Clinion's eTMF utilizes industry-standard DIA TMF Reference Models for a user-friendly experience, allowing for ef…

Explore the comprehensive guide to Whole Slide Imaging scanners, covering benefits, applications, and technology. Read the blog to know more.
 Whole Slide Imaging: Whole slide imaging, commonly known as virtual microscopy, revolutionizes the way pathology specimens are analyzed by digitizing entire tissue slides for comprehensive examination. This technology involves scanning various whole slides digitally in high resolution, stitching together images derived from each field of view across the complete microscopy slide using specialized software. The result is a single digital image file that can be stored safely for archiving and documentation, benefiting the consulting and teaching industries. This cutting-edge technology allows pathologists to view high-resolution images of entire t…

Medical devices encompass simple devices such as tongue depressors, bandages, and syringes to imaging devices (ultrasound and CT scanners), implantable devices (pacemakers), and medical equipment. The emergence and technological advancements in of data analytics, artificial intelligence (AI), and increased internet connectivity and accessibility has led to the widespread use of Software as a Medical Device (SaMD) in diseases prevention, diagnosis, and treatment.
Medical devices encompass simple devices such as tongue depressors, bandages, and syringes to imaging devices (ultrasound and CT scanners), implantable devices (pacemakers), and medical equipment. The emergence and technological advancements in of data analytics, artificial intelligence (AI), and increased internet connectivity and…

In today’s competitive clinical research landscape, seamless EDC-CTMS integration is not simply a convenience; it’s a strategic imperative
Clinical trials are complex endeavours that rely on meticulous data collection, efficient communication, and rigorous oversight. Two critical software systems underpin these needs: Electronic Data Capture (EDC) and Clinical Trial Management Systems (CTMS). This post explores why seamless integration between EDC and CTMS is paramount for effective trial management. What are EDC and CTMS? EDC (Electronic Data Capture): Imagine a digital filing cabinet for clinical trial data. EDC systems streamline participant data collection, ensuring accuracy and regulatory compliance. CTMS (Clinical Trial Management System): Think of CTMS system as t…

In 2020, the global landscape changed dramatically with the advent of COVID-19. The fatal virus strain soon infected millions of people worldwide, forcing everyone to live a masked life that became limited to their homes.
Problem Statement In 2020, the global landscape changed dramatically with the advent of COVID-19. The fatal virus strain soon infected millions of people worldwide, forcing everyone to live a masked life that became limited to their homes. Bharat Biotech is one of India’s leading Biotech companies and when India got hit by the COVID-19 pandemic, the company started looking for a proven and easy-to-use system that could accelerate COVID vaccine trials. Bharat Biotech’s Covaxin, one of the first COVID-19 vaccines developed by an Indian company, was approved to enter Phase 1…

Clinion's Clinical Trial Management System (CTMS) gives enhanced visibility into all aspects of the clinical trial process - from study plan, Remote monitoring, and Clinical data management.
Clinion CTMS is an integrated Clinical Trial Management System (CTMS) designed to give Contract Research Organizations (CROs) and Sponsors greater visibility and control over their clinical trials. Here's a breakdown of its key features and benefits: Real-time Visibility: Gain a comprehensive view of your entire trial at any time. This allows for faster decision-making and course correction, potentially accelerating study timelines. Reduced Trial Costs: Clinion CTMS helps streamline workflows, automate tasks, and optimize spending. This can lead to significant cost savings by minimizing redun…

Clinical Data Management (CDM) has drastically transformed over the years, proactively adapting to technological advancements, changing regulations, and the growing complexity of clinical trials. In this article, we explore the milestones that have shaped the face of CDM over the years and discuss what the future could hold for the role of CDM in clinical research.
Clinical Data Management (CDM) has drastically transformed over the years, proactively adapting to technological advancements, changing regulations, and the growing complexity of clinical trials. In this article, we explore the milestones that have shaped the face of CDM over the years and discuss what the future could hold for the role of CDM in clinical research. Read the full article on PharmiWeb.Jobs.

Optimize your clinical trials with Clinion RTSM software the easy-to-use and innovative solution that puts patient safety and accurate randomization first
We at Clinion are excited to share our all-in-one Randomization and Trial Supply Management (RTSM) software designed to streamline clinical trial operations! Effortless Integration: Our RTSM seamlessly integrates with our EDC platform. Randomize patients and assign investigational product kits directly within the same system, eliminating the need to switch between applications and reducing the risk of data entry errors. Flexible Randomization Power: Clinion's RTSM caters to diverse study designs. Whether you require simple randomization or complex stratified/minimization approaches, our software can handle it! Real-ti…

AI is transforming medical coding by improving coding accuracy. In this blog, we’ll explore what this transformation means for clinical trial organizations.
Accuracy in medical coding is a vital aspect in aiding clinical trial operation success. It has presented an excellent opportunity for medical coders, working hand-in-hand with AI-enhanced computer-assisted coding systems, to quickly identify and validate the correct codes. Using natural language processing (NLP) and advanced Machine Learning algorithms, AI is transforming medical coding by improving coding accuracy. In this blog, we’ll explore what this transformation means for clinical trial organizations. What is Medical Coding? Medical coding is a critical process that involves assigning standardized codes to medical terms in clinic…

Clinion electronic data capture (EDC) software uses AI to simplify Study Build and set up your study in days instead of weeks with an easy-to-use interface
The Freedom And Flexibility To Built Studies On Your Own Clinion Electronic Data Capture (EDC) Software uses AI and Automation to simplify Study Build, Data Capture and Clinical Data Management (CDM). With advanced features like Medical Coding Automation, External Data Load, Visit Scheduling, Bulk locks, CRF versioning as part of a standard package Clinion makes things simpler for its users. Integrate Clinion Electronic Data Capture (EDC) Software with Clinion CTMS, IWRS/RTSM, and ePRO/eCOA for true end-to-end support of your Study, obviating the hassles of data reconciliation while dealing with multiple eCl…

A Clinical Research Coordinator (CRC) is a specialised research professional who works under the direction of a Clinical Principal Investigator (PI). They play an important role in conducting and managing clinical trials, providing outcomes that shape medical advances in areas such as preventative care, cures for diseases, and immunisations.
A Clinical Research Coordinator (CRC) is a specialised research professional who works under the direction of a Clinical Principal Investigator (PI). They play an important role in conducting and managing clinical trials, providing outcomes that shape medical advances in areas such as preventative care, cures for diseases, and immunisations. The CRC is primarily responsible for overseeing clinical trials or studies that test the effectiveness of new dru…

From nurturing a positive work culture to empowering and developing your people for success, Pioneer Group sets out some top tips for building a high-performance team as a life science company.
When it comes to recruitment, the life sciences industry is undoubtedly highly competitive. With demand for skilled professionals often outpacing the supply, attracting (and retaining) qualified candidates with the right expertise can be a significant challenge for many life science companies. From nurturing a positive work culture to empowering and developing your people for success, Pioneer Group sets out some top tips for building a high-performance team as a life science company. Invest in Graduate Programmes Investing in graduate outreach can help to bridge the skills gap in life sciences, and…

Learn Clinical Research, Clinical Data Management Training in Bangalore. (CDM)Clinical Data Management Online Classes 2024 for Life Science graduates Industry Expert.
Career in Clinical Data Management   In the rapidly evolving landscape of healthcare, the role of Clinical Data Management (CDM) is gaining prominence as a crucial driver of innovation and progress. This blog explores the future of healthcare through the lens of professionals in Clinical Data Management, offering valuable career perspectives and insights into the transformative impact of data in the industry.  Opportunities: Career opportunities in Clinical Data Management are diverse and rewarding, career offering as Clinical Data Coordinator which is an Entry-level role, responsible for data entry, verification, an…

Clinical Research Organisations (CROs) play a crucial role in advancing medical knowledge and therapeutic innovations. As vital intermediaries between pharmaceutical and biotechnology companies, healthcare professionals, and regulatory bodies, CROs help facilitate the clinical development of new drugs, devices, and treatments.
Clinical Research Organisations (CROs) play a crucial role in advancing medical knowledge and therapeutic innovations. As vital intermediaries between pharmaceutical and biotechnology companies, healthcare professionals, and regulatory bodies, CROs help facilitate the clinical development of new drugs, devices, and treatments. In this article, we explore the multifaceted functions of modern CROs, highlighting the significant impact they have on shaping the future of h…

● At the 17th International Conference on Advanced Technologies and Treatments for Diabetes (ATTD) in Florence, Italy, Roche shared recent accuracy data for its new Accu-Chek SmartGuide solution for real-time continuous glucose monitoring (rtCGM). ● International experts discussed how a novel CGM solution using prediction capabilities can address unmet needs of people with diabetes at the Roche symposium. ● The presented study results underlined the accurate and safe performance of the solution.
Roche (SIX: RO, ROG; OTCQX: RHHBY) presented the latest data on its novel solution for continuous glucose monitoring. The solution consists of a CGM sensor and two apps designed to display current glucose values and predictions over 30 minutes and two hours. In addition, it features a risk predi…

The Mental Health Screening market is projected to reach USD 1.8 billion by 2029 from USD 0.9 billion in 2023, at a CAGR 12.2% from 2023 to 2029
According to a new report by MarketsandMarkets™ – Mental Health Screening Market in terms of revenue was estimated to be worth $0.9 billion in 2023 and is poised to reach $1.8 billion by 2029, growing at a CAGR of 12.2% from 2023 to 2029. The growth in the Mental Health Screening market is driven by the growing geriatric population and subsequent increase in the prevalence of mental disorders, rising awareness of mental health issues, technological advancements, and the increasing focus on remote monitoring. The adoption of mental health screening tools is also expected to increase with the integration with wearable technologies and the…

In terms of revenue, the global clinical trials market was estimated to be worth $48.2 billion in 2023 and is expected to reach $73.2 billion by 2028, growing at a CAGR of 8.7%. In this article, we’ve rounded up 9 of the top Clinical Research Organisations (CROs) in the world, highlighting the key drivers of this growth.
In terms of revenue, the global clinical trials market was estimated to be worth $48.2 billion in 2023 and is expected to reach $73.2 billion by 2028, growing at a CAGR of 8.7%. In this article, we’ve rounded up 9 of the top Clinical Research Organisations (CROs) in the world, highlighting the key drivers of this growth. Read the full article on PharmiWeb.Jobs.

Embarking on a systematic literature review is a critical step in evidence synthesis, providing a foundation for robust decision-making in the healthcare landscape. As with most things, there are ways to cut corners on systematic reviews. Sometimes there are true efficiencies to be made. Yet, all compromises have consequences. In this article, we delve into 11 common problems that may arise when cost-cutting compromises the quality of your systematic literature review.
1. Choosing the wrong type of systematic review methodology Selecting the wrong type of methodology for your review can have profound implications. A robust, gold standard Cochrane methodology involves two reviewers at all stages of the review, to avoid bias in the identification and presentation of the evidence, and ensur…

CD73, also known as ecto-5′-nucleotidase, is a groundbreaking immunoinhibitory protein that assumes a pivotal role in tumor growth and metastasis. Its primary function revolves around converting extracellular ATP into immunosuppressive adenosine, working in tandem with CD39 within normal tissues to curtail excessive immune reactions. However, this mechanism is often hijacked by tumors, utilizing CD73 to foster an adenosinergic process that shields them from immune assaults.
Exploring the Structure and Function of CD73 The CD73 gene finds its home in the 6q14.3 region of human chromosome 6, encoding a protein comprised of 549 amino acid residues. CD73 functions as a glycosylphospholipase, residing on the cell membrane surface and engaging with the extracellular matrix through its extracellul…

AI in drug discovery has revolutionized the pharmaceutical industry by accelerating the process of drug development, making it more efficient and cost-effective. It combines advanced algorithms, machine learning, and big data analysis to expedite the identification of potential drug candidates and optimize their properties.
One significant area where AI shines is in predicting molecular properties and interactions. Machine learning models can analyze vast datasets of molecular structures, biological data, and chemical properties to predict how a compound might interact with specific targets in the body. This predictive power expedites the identification of potential drug candidates, saving considerable time and resources in the initial stages of drug discovery. Additionally, AI enables the…